Structure of PDB 4erm Chain B Binding Site BS01
Receptor Information
>4erm Chain B (length=734) Species:
83333
(Escherichia coli K-12) [
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NLLVTKRDGSTERINLDKIHRVLDWAAEGLHNVSISQVELRSHIQFYDGI
KTSDIHETIIKAAADLISRDAPDYQYLAARLAIFHLRKKAYGQFEPPALY
DHVVKMVEMGKYDNHLLEDYTEEEFKQMDTFIDHDRDMTFSYAAVKQLEG
KYLVQNRVTGEIYESAQFLYILVAACLFSNYPRETRLQYVKRFYDAVSTF
KISLPTPIMSGVRTPTRQFSSCVLIECGDSLDSINATSSAIVKYVSQRAG
IGINAGRIRALGSPIRGGEAFHTGCIPFYKHFQTAVKSCSQGGVRGGAAT
LFYPMWHLEVESLLVLKNNRGVEGNRVRHMDYGVQINKLMYTRLLKGEDI
TLFSPSDVPGLYDAFFADQEEFERLYTKYEKDDSIRKQRVKAVELFSLMM
QERASTGRIYIQNVDHCNTHSPFDPAIAPVRQSNLCLEIALPTKPLNDVN
DENGEIALCTLSAFNLGAINNLDELEELAILAVRALDALLDYQDYPIPAA
KRGAMGRRTLGIGVINFAYYLAKHGKRYSDGSANNLTHKTFEAIQYYLLK
ASNELAKEQGACPWFNETTYAKGILPIDTYKKDLDTIANEPLHYDWEALR
ESIKTHGLRNSTLSALMPSETSSQISNATNGIEPPRGYVSIKASKDGILR
QVVPDYEHLHDAYELLWEMPGNDGYLQLVGIMQKFIDQSISANTNYDPSR
FPSGKVPMQQLLKDLLTAYKFGVKTLYYQNTRDG
Ligand information
Ligand ID
DTP
InChI
InChI=1S/C10H16N5O12P3/c11-9-8-10(13-3-12-9)15(4-14-8)7-1-5(16)6(25-7)2-24-29(20,21)27-30(22,23)26-28(17,18)19/h3-7,16H,1-2H2,(H,20,21)(H,22,23)(H2,11,12,13)(H2,17,18,19)/t5-,6+,7+/m0/s1
InChIKey
SUYVUBYJARFZHO-RRKCRQDMSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)[C@H]3C[C@@H]([C@H](O3)CO[P@](=O)(O)O[P@@](=O)(O)OP(=O)(O)O)O)N
CACTVS 3.341
Nc1ncnc2n(cnc12)[CH]3C[CH](O)[CH](CO[P](O)(=O)O[P](O)(=O)O[P](O)(O)=O)O3
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)C3CC(C(O3)COP(=O)(O)OP(=O)(O)OP(=O)(O)O)O)N
CACTVS 3.341
Nc1ncnc2n(cnc12)[C@H]3C[C@H](O)[C@@H](CO[P@@](O)(=O)O[P@](O)(=O)O[P](O)(O)=O)O3
ACDLabs 10.04
O=P(O)(O)OP(=O)(O)OP(=O)(O)OCC3OC(n2cnc1c(ncnc12)N)CC3O
Formula
C10 H16 N5 O12 P3
Name
2'-DEOXYADENOSINE 5'-TRIPHOSPHATE
ChEMBL
CHEMBL335538
DrugBank
DB03222
ZINC
ZINC000008215662
PDB chain
4erm Chain B Residue 801 [
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Receptor-Ligand Complex Structure
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PDB
4erm
Tangled up in knots: structures of inactivated forms of E. coli class Ia ribonucleotide reductase.
Resolution
3.95 Å
Binding residue
(original residue number in PDB)
V7 K9 R10 I17 N18 K21 T55 H59 F87
Binding residue
(residue number reindexed from 1)
V4 K6 R7 I14 N15 K18 T52 H56 F84
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
C225 N437 C439 E441 C462 Y730 Y731
Catalytic site (residue number reindexed from 1)
C222 N434 C436 E438 C459 Y727 Y728
Enzyme Commision number
1.17.4.1
: ribonucleoside-diphosphate reductase.
Gene Ontology
Molecular Function
GO:0004748
ribonucleoside-diphosphate reductase activity, thioredoxin disulfide as acceptor
GO:0005515
protein binding
GO:0005524
ATP binding
GO:0016491
oxidoreductase activity
GO:0042802
identical protein binding
GO:0044183
protein folding chaperone
Biological Process
GO:0006457
protein folding
GO:0009185
ribonucleoside diphosphate metabolic process
GO:0009263
deoxyribonucleotide biosynthetic process
GO:0009265
2'-deoxyribonucleotide biosynthetic process
GO:0015949
nucleobase-containing small molecule interconversion
Cellular Component
GO:0005829
cytosol
GO:0005971
ribonucleoside-diphosphate reductase complex
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:4erm
,
PDBe:4erm
,
PDBj:4erm
PDBsum
4erm
PubMed
22727814
UniProt
P00452
|RIR1_ECOLI Ribonucleoside-diphosphate reductase 1 subunit alpha (Gene Name=nrdA)
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